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Ammonia → 2,6-Dichloropyrimidine-4-carboxamide

HRID 1752388
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HRID 1752388 반응식
[Cl:1][C:2]1[N:7]=[C:6]([C:8](Cl)=[O:9])[CH:5]=[C:4]([Cl:11])[N:3]=1.N.O1CCOCC1.CC[N:21](C(C)C)C(C)C>CCOCC>[Cl:1][C:2]1[N:7]=[C:6]([C:8]([NH2:21])=[O:9])[CH:5]=[C:4]([Cl:11])[N:3]=1
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참가 물질

6

반응물 4

HCID 222AmmoniaHCID 312751,4-DioxaneHCID 81531DiisopropylethylamineHCID 110311332,6-dichloropyrimidine-4-carbonyl Chloride

생성물 1

HCID 2411282,6-Dichloropyrimidine-4-carboxamide수율 41.1%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

To a solution of 2,6-dichloropyrimidine-4-carbonyl chloride (26.13 g, 123.6 mmol) in Et2O (500 mL) was added a mixture of 0.5M ammonia in dioxane (250 mL, 125 mmol) and iPr2NEt (22 mL, 126 mmol) dropwise over approximately 50 minutes. After stirring overnight the reaction was concentrated in vacuo to a residue and chromatographed over silica gel with 10-50% EtOAc in hexanes. The product fractions were evaporated in vacuo, and the resulting solid residue triturated with 10 mL 10% EtOAc/hexanes and filtered to give 2,6-dichloropyrimidine-4-carboxamide as an orange crystalline solid (9.743 g, 50.74 mmol, 41% yield). LC/MS: m/z=192.2 [M+H]+, 1H NMR (400 MHz, DMSO-d6): 8.40 (1H, br s), 8.16 (1H, br s), 8.10 (1H, s).

후처리

  1. concentrationwas concentrated in vacuo to a residue
  2. customchromatographed over silica gel with 10-50% EtOAc in hexanes
  3. customThe product fractions were evaporated in vacuo
  4. customthe resulting solid residue triturated with 10 mL 10% EtOAc/hexanes
  5. filtrationfiltered

출처 및 근거

ORD 기록
ord-ba80fda56709426fb6d2230b453c3d22
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09163008B2

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